Clinical Research Analyst – Senior

Qori Gente e Gestão

Senior Clinical Research Analyst responsible for managing clinical studies, documentation, and regulatory compliance. Collaborating with investigators and internal teams to ensure project success in a pharmaceutical industry.

Posted 8/1/2026full-timeSão Paulo • 🇧🇷 BrazilSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical study operations, including regulatory documentation and interaction with stakeholders. Proficient in utilizing clinical research systems such as CRF and eTMF/TMF to ensure project progress.

Highest-signal resume keywords

Clinical Study Operations ManagementRegulatory Documentation ManagementCRF FamiliarityETMF/TMF KnowledgeStakeholder Interaction

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study OperationsRegulatory DocumentationCRFETMFTMF

Soft Skills

CommunicationCollaboration

Tools & Technologies

Clinical Research Systems

Industry Keywords

Clinical ResearchStudy Start-UpOperational Management

About the role

Key responsibilities & impact

Manage and oversee clinical study operations from start to finish:
Participate in study start-up and operational management.
Manage regulatory and study documentation, including working knowledge of CRF, eTMF/TMF and other systems used in clinical research.
Interact with investigators, physicians and various internal departments to ensure proper progress of projects.

Requirements

What you’ll need

Bachelor's degree or higher;
Fluent in English;
Experience in clinical study operations;
Familiarity with CRF, eTMF/TMF and relevant clinical systems.

Benefits

Comp & perks

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